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Radiocarbon analysis in an Alpine ice core: record of anthropogenic and biogenic contributions to carbonaceous aerosols in the past (1650–1940)

机译:高山冰芯中的放射性碳分析:过去人类活动和生物活动对碳质气溶胶的贡献记录(1650年-1940年)

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Long-term concentration records of carbonaceous particles (CP) are ofincreasing interest in climate research due to their not yet completelyunderstood effects on climate. Nevertheless, only poor data on theirconcentrations and sources before the 20th century are available. Wepresent a first long-term record of organic carbon (OC) and elemental carbon(EC) concentrations – the two main fractions of CP – along with thecorresponding fraction of modern carbon (fM) derived from radiocarbon(14C) analysis in ice. This allows a distinction and quantification ofnatural (biogenic) and anthropogenic (fossil) sources in the past. CP wereextracted from an ice archive, with resulting carbon quantities in themicrogram range. Analysis of 14C by accelerator mass spectrometry (AMS)was therefore highly demanding. We analysed 33 samples of 0.4 to 1 kg icefrom a 150.5 m long ice core retrieved at Fiescherhorn glacier in December2002 (46°33'3.2" N, 08°04'0.4" E; 3900 m a.s.l.). Samples were takenfrom bedrock up to the firn/ice transition, covering the time period1650–1940 and thus the transition from the pre-industrial to the industrialera. Before ~1850, OC was approaching a purely biogenic origin with amean concentration of 24 μg kg−1 and a standard deviation of 7 μg kg−1.In 1940, OC concentration was about a factor of 3 higherthan this biogenic background, almost half of it originating fromanthropogenic sources, i.e. from combustion of fossil fuels. The biogenic ECconcentration was nearly constant over the examined time period with 6 μg kg−1and a standard deviation of 1 μg kg−1. In 1940, theadditional anthropogenic input of atmospheric EC was about 50 μg kg−1.
机译:碳质颗粒(CP)的长期浓度记录由于对气候的影响尚未完全被人们理解,因此在气候研究中越来越受到关注。然而,只有20世纪之前关于其浓度和来源的不良数据。我们提供了第一个长期的有机碳(OC)和元素碳(EC)浓度(CP的两个主要部分)以及相应的源自放射性碳的现代碳(f M )分数的长期记录。冰中的 14 C)分析。这样可以对过去的自然(生物源)和人为(化石)源进行区分和定量。从冰档案中提取CP,得到的碳量在微克范围内。因此,通过加速器质谱(AMS)分析 14 C的要求很高。我们分析了2002年12月在菲斯霍恩冰川(46°33'3.2“ N,08°04'0.4” E; 3900 m a.s.l.)从150.5 m长的冰芯中提取的33个0.4-1 kg冰样品。样品是从基岩一直到冰/冰的过渡期采集的,涵盖了1650至1940年的时间段,也就是从工业化到工业化的过渡期。约1850年之前,OC接近纯生物起源,安曼浓度为24μgkg -1 ,标准偏差为7μgkg -1 。1940年,OC浓度比这个生物背景高约3倍,其中几乎一半来自人为来源,即化石燃料的燃烧。在检查的时间段内,生物EC浓度几乎恒定,为6μgkg -1 ,标准偏差为1μgkg -1 。 1940年,大气EC的额外人为输入约为50μgkg -1

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